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| 38036523 | Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. | Nat Commun | 2023 |
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| 37471144 | The predominant PAR4 variant in individuals of African ancestry worsens murine and human stroke outcomes. | J Clin Invest | 2023 |
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| 36444934 | Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease. | Hum Mol Genet | 2023 |
| 36540998 | Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index. | Pac Symp Biocomput | 2023 |
| 34672390 | Mendelian randomization in the multivariate general linear model framework. | Genet Epidemiol | 2022 |
| 35710995 | Genome-wide polygenic score to predict chronic kidney disease across ancestries. | Nat Med | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
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| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
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| 36334310 | Association of a Multiancestry Genome-Wide Blood Pressure Polygenic Risk Score With Adverse Cardiovascular Events. | Circ Genom Precis Med | 2022 |
| 36240095 | Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke. | Neurology | 2022 |
| 36292585 | Differentially Methylated DNA Regions and Left Ventricular Hypertrophy in African Americans: A HyperGEN Study. | Genes (Basel) | 2022 |
| 35886043 | Genetic Contributors of Efficacy and Adverse Metabolic Effects of Chlorthalidone in African Americans from the Genetics of Hypertension Associated Treatments (GenHAT) Study. | Genes (Basel) | 2022 |
| 36193739 | Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney Function. | Hypertension | 2022 |
| 36220816 | Whole genome sequence analysis of blood lipid levels in >66,000 individuals. | Nat Commun | 2022 |
| 35100591 | APOL1 Risk Variants Associated with Serum Albumin in a Population-Based Cohort Study. | Am J Nephrol | 2022 |
| 33100131 | Epigenome-wide association study identifies DNA methylation sites associated with target organ damage in older African Americans. | Epigenetics | 2021 |
| 33720349 | Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. | Genetics | 2021 |
| 33679876 | Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify <i>MYRIP</i>, <i>TRAPPC11</i>, and <i>SLC27A6</i> of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population. | Front Genet | 2021 |
| 33821945 | DNA Methylation and Blood Pressure Phenotypes: A Review of the Literature. | Am J Hypertens | 2021 |
| 33812378 | Age and sex are associated with the plasma lipidome: findings from the GOLDN study. | Lipids Health Dis | 2021 |
| 33637890 | Genetic correlations between traits associated with hyperuricemia, gout, and comorbidities. | Eur J Hum Genet | 2021 |
| 34992631 | Genetic Contributors of Incident Stroke in 10,700 African Americans With Hypertension: A Meta-Analysis From the Genetics of Hypertension Associated Treatments and Reasons for Geographic and Racial Differences in Stroke Studies. | Front Genet | 2021 |
| 34468868 | Lipid Phenotypes and DNA Methylation: a Review of the Literature. | Curr Atheroscler Rep | 2021 |
| 34611638 | High triglyceride to HDL cholesterol ratio is associated with increased coronary heart disease among White but not Black adults. | Am J Prev Cardiol | 2021 |
| 34780523 | A 6-CpG validated methylation risk score model for metabolic syndrome: The HyperGEN and GOLDN studies. | PLoS One | 2021 |
| 34397689 | Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study. | Medicine (Baltimore) | 2021 |
| 34836252 | Genomics of Postprandial Lipidomics in the Genetics of Lipid-Lowering Drugs and Diet Network Study. | Nutrients | 2021 |
| 34183656 | A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids. | Nat Commun | 2021 |
| 34214102 | Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. | PLoS One | 2021 |
| 34231218 | Adverse Cardiovascular Outcomes and Antihypertensive Treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies. | Clin Pharmacol Ther | 2021 |
| 32299504 | Gout is associated with an increased risk for incident heart failure among older adults: the REasons for Geographic And Racial Differences in Stroke (REGARDS) cohort study. | Arthritis Res Ther | 2020 |
| 31985870 | Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African Americans. | J Thromb Haemost | 2020 |
| 33339817 | Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. | Nat Commun | 2020 |
| 33121163 | Genetic-Based Hypertension Subtype Identification Using Informative SNPs. | Genes (Basel) | 2020 |
| 32930325 | Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A. | Am J Clin Nutr | 2020 |
| 32586392 | A lipidome-wide association study of the lipoprotein insulin resistance index. | Lipids Health Dis | 2020 |
| 32840624 | Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples. | J Nutr | 2020 |
| 29788187 | Distracted Driving and Risk of Crash or Near-Crash Involvement Among Older Drivers Using Naturalistic Driving Data With a Case-Crossover Study Design. | J Gerontol A Biol Sci Med Sci | 2019 |
| 31869403 | Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. | PLoS Genet | 2019 |
| 30239588 | Integrating hypertension phenotype and genotype with hybrid non-negative matrix factorization. | Bioinformatics | 2019 |